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Effect of Ascorbate on the Cyanide-Scavenging Capability of Cobalt(III) meso-Tetra(4-N-methylpyridyl)porphine Pentaiodide: Deactivation by Reduction?

机译:抗坏血酸对内消旋钴(III)-四(4-N-甲基吡啶基)卟啉戊二酰亚胺氰化物清除能力的影响:还原失活吗?

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摘要

The Co(III)-containing water-soluble metalloporphyrin cobalt(III) meso-tetra(4-N-methylpyridyl)porphine pentaiodide (CoIIITMPyP) is a potential cyanide-scavenging agent. The rate of reduction of CoIIITMPyP by ascorbate is facile enough that conversion to the Co(II)-containing CoIITMPyP should occur within minutes at prevailing in vivo levels of the reductant. It follows that any cyanide-decorporating capability of the metalloporphyrin should depend more on the cyanide-binding characteristics of CoIITMPyP than those of the administered form, CoIIITMPyP. Addition of cyanide to buffered aqueous solutions of CoIITMPyP (pH 7.4, 25–37 °C) results in quite rapid (k2 = ~103 M−1 s−1) binding/substitution of cyanide anion in the two available axial positions with high affinity (K′β = 1010 to 1011). Electron paramagnetic resonance spectroscopic measurements and cyclic voltammetry indicate that cyanide induces oxidation to the Co(III)-containing dicyano species. The constraints that these observations put on plausible mechanisms for the reaction of CoIITMPyP with cyanide are discussed. Experiments in which CoIIITMPyP and cyanide were added to freshly drawn mouse blood showed the same sequence of reactions (metalloporphyrin reduction → cyanide binding/substitution → reoxidation) to occur. Therefore, in cyanide-scavenging applications with this metalloporphyrin, we should be taking advantage of both the improved rate of ligand substitution at Co(II) compared to that at Co(III) and the increased affinity of Co(III) for anionic ligands compared to that of Co(II). Finally, using an established sublethal mouse model for cyanide intoxication, CoIIITMPyP, administered either 5 min before (prophylaxis) or 1 min after the toxicant, is shown to have very significant antidotal capability. Possible explanations for the results of a previous contradictory study, which failed to find any prophylactic effect of CoIIITMPyP toward cyanide intoxication, are considered.
机译:含钴(III)的水溶性金属卟啉钴(III)内-四(4-N-甲基吡啶基)卟啉五氧化二钴(Co III TMPyP)是一种潜在的氰化物清除剂。抗坏血酸还原Co III TMPyP的速率足够容易,以至于在体内主要水平下,几分钟之内即可转化为含Co(II)的Co II TMPyP。还原剂。由此可见,金属卟啉的任何氰化物分解能力应更多地依赖于Co III TMPyP的氰化物结合特性,而不是给药形式的Co III TMPyP。将氰化物添加到Co II TMPyP的缓冲水溶液(pH 7.4,25–37°C)中会非常快(k2 =〜10 3 M -在两个可用的轴向位置以高亲和力(K′β = 10 10 到10 )1 s -1 )结合/取代氰化物阴离子11 )。电子顺磁共振光谱测量和循环伏安法表明,氰化物可诱导氧化成含Co(III)的双氰基物质。讨论了这些观察对Co TMPyP与氰化物反应的合理机理的约束。将Co III PyP和氰化物添加到新鲜抽取的小鼠血液中的实验表明,发生了相同的反应顺序(金属卟啉还原→氰化物结合/取代→再氧化)。因此,在用这种金属卟啉清除氰化物的应用中,我们应该既利用Co(II)的配体取代率比Co(III)的提高,又利用Co(III)对阴离子配体的亲和力提高相当于Co(II)。最后,使用建立的氰化物中毒亚致死小鼠模型,Co(sup> III TMPyP,在有毒物质之前(预防)5分钟(预防)或在毒害物质之后1分钟给药,具有很强的解毒能力。考虑了以前的一项矛盾研究结果的可能解释,该研究未能发现Co III TMPyP对氰化物中毒有任何预防作用。

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